pseudohypoaldosteronism type 2B
MONDO:0013777Mondo
Findings
No curated finding names pseudohypoaldosteronism type 2B yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any pseudohypoaldosteronism type 2 in which the cause of the disease is a mutation in the WNK4 gene.
Definition from the Mondo Disease Ontology (MONDO:0013777), read 2026-09-29. CC BY 4.0.
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- WNK4HGNC:14544
- Definitive · ClinGen · Autosomal dominant · 2026
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2021
- Strong · PanelApp Australia · Autosomal dominant · 2025
- Moderate · Ambry Genetics · Autosomal dominant · 2023
Where it sits
- A kind of
Other names
3 names
Resolves to: pseudohypoaldosteronism type 2B
- Also called
- PHA2Bpseudohypoaldosteronism type 2 caused by mutation in WNK4WNK4 pseudohypoaldosteronism type 2